Spatiotemporal Imaging of Zinc Ions in Zebrafish Live Brain Tissue Enabled by Fluorescent Bionanoprobes

Author:

Jarosova Romana12,Woolfolk Sarah K.34,Martinez-Rivera Noraida5ORCID,Jaeschke Mathew W.36,Rosa-Molinar Eduardo57ORCID,Tamerler Candan346ORCID,Johnson Michael A.1ORCID

Affiliation:

1. Department of Chemistry and R.N. Adams Institute for Bioanalytical Chemistry, University of Kansas, Lawrence, KS 66045, USA

2. UNESCO Laboratory of Environmental Electrochemistry, Department of Analytical Chemistry, Charles University, 12843 Prague 2, Czech Republic

3. Institute for Bioengineering Research, University of Kansas, Lawrence, KS 66045, USA

4. Bioengineering Program, University of Kansas, Lawrence, KS 66045, USA

5. Microscopy and Analytical Imaging Research Resource Core Laboratory, University of Kansas, Lawrence, KS 66045, USA

6. Department of Mechanical Engineering, University of Kansas, Lawrence, KS 66045, USA

7. Department of Pharmacology & Toxicology, University of Kansas, Lawrence, KS 66045, USA

Abstract

The zebrafish is a powerful model organism to study the mechanisms governing transition metal ions within whole brain tissue. Zinc is one of the most abundant metal ions in the brain, playing a critical pathophysiological role in neurodegenerative diseases. The homeostasis of free, ionic zinc (Zn2+) is a key intersection point in many of these diseases, including Alzheimer’s disease and Parkinson’s disease. A Zn2+ imbalance can eventuate several disturbances that may lead to the development of neurodegenerative changes. Therefore, compact, reliable approaches that allow the optical detection of Zn2+ across the whole brain would contribute to our current understanding of the mechanisms that underlie neurological disease pathology. We developed an engineered fluorescence protein-based nanoprobe that can spatially and temporally resolve Zn2+ in living zebrafish brain tissue. The self-assembled engineered fluorescence protein on gold nanoparticles was shown to be confined to defined locations within the brain tissue, enabling site specific studies, compared to fluorescent protein-based molecular tools, which diffuse throughout the brain tissue. Two-photon excitation microscopy confirmed the physical and photometrical stability of these nanoprobes in living zebrafish (Danio rerio) brain tissue, while the addition of Zn2+ quenched the nanoprobe fluorescence. Combining orthogonal sensing methods with our engineered nanoprobes will enable the study of imbalances in homeostatic Zn2+ regulation. The proposed bionanoprobe system offers a versatile platform to couple metal ion specific linkers and contribute to the understanding of neurological diseases.

Funder

National Institute of Neurological Disorders and Stroke of the National Institutes of Health

National Institute of General Medical Sciences of the National Institutes of Health

University of Kansas College of Liberal Arts and Sciences

NSF-CHE program

NSF

Charles University in Prague

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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